Suppr超能文献

表现为巨大腹膜后脓肿的肾炎性肌纤维母细胞瘤。

Renal inflammatory myofibroblastic tumour presenting with a large retroperitoneal abscess.

作者信息

Bandara Ginimal Bandaralage Kavinda Deshapriya, Jayarajah Umesh, Rodrigo Vitharanage Srimantha Dewsiri

机构信息

Department of Surgery, District General Hospital, Chilaw, Sri Lanka.

出版信息

SAGE Open Med Case Rep. 2022 Apr 4;10:2050313X221089484. doi: 10.1177/2050313X221089484. eCollection 2022.

Abstract

Inflammatory myofibroblastic tumour arising from the kidney is a rare occurrence. In this case report, we present a rare case of inflammatory myofibroblastic tumour arising from the kidney diagnosed after the presentation with a large retroperitoneal abscess for the first time in literature. A 55-year-old woman with diabetes mellitus presented to us with painful lump in the left lumbar region of the back for 1-week duration. On examination, there was a firm, diffuse lump in the left lumbar region of the back. Her inflammatory markers were high, but the serum creatinine and blood urea were within the normal range. Abdominal ultrasonography showed a distorted left kidney with a heterogeneous mass consisting cystic and solid components measuring approximately 7 × 9 × 8 cm in size. A contrast-enhanced computed tomography scan showed an 11 × 9 × 9 cm-sized low-density mass posterior to the left kidney with multiple contrast-enhancing septations which appeared posterior to but separate from the left kidney within the left renal fascia. There was breeching of the Gerota's fascia with extension posteriorly up to subcutaneous tissue. Since the radiological opinion was in favour of a complex perinephric abscess, open drainage of the abscess was performed after failed attempts of ultrasound-guided drainage. The biopsy of the abscess wall was suggestive of a renal cell carcinoma and radical nephrectomy was planned. Due to tumour invasion, the radical nephrectomy was combined with a splenectomy and the specimen sent for histology. It showed an inflammatory myofibroblastic tumour or pseudotumour with the periphery showing ulceration and abscess formation. The patient had an uneventful recovery following surgery. Thus, we report the first case of renal inflammatory myofibroblastic tumour presenting with a large retroperitoneal abscess extending to the subcutaneous tissue plane. Final diagnosis was made only after radical surgery which was curative.

摘要

肾脏炎性肌纤维母细胞瘤极为罕见。在本病例报告中,我们呈现了一例罕见的肾脏炎性肌纤维母细胞瘤,该病例首次在文献中报道,患者最初表现为巨大的腹膜后脓肿。一名55岁的糖尿病女性患者因左腰背部疼痛性肿块前来就诊,病程1周。体格检查发现左腰背部有一个质地坚硬、边界不清的肿块。她的炎症指标升高,但血清肌酐和血尿素在正常范围内。腹部超声显示左肾形态失常,有一个大小约为7×9×8cm的囊实性混合性肿块。增强计算机断层扫描显示左肾后方有一个大小为11×9×9cm的低密度肿块,有多个强化分隔,位于左肾筋膜内左肾后方但与左肾分离。肾周筋膜破裂,炎症向后延伸至皮下组织。由于影像学检查结果提示为复杂性肾周脓肿,在超声引导下引流失败后,进行了脓肿切开引流。脓肿壁活检提示肾细胞癌,遂计划行根治性肾切除术。由于肿瘤侵犯,根治性肾切除术联合脾切除术,并将标本送检做组织学检查。结果显示为炎性肌纤维母细胞瘤或假肿瘤,周边有溃疡和脓肿形成。患者术后恢复顺利。因此,我们报道了首例以巨大腹膜后脓肿延伸至皮下组织平面为表现的肾脏炎性肌纤维母细胞瘤病例。最终诊断仅在根治性手术后得以明确,手术具有治愈效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c9/8984842/e4ec9b1749af/10.1177_2050313X221089484-fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验